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A synthetic pathway to diquinane and angular triquinane systems via an iron carbonyl promoted tandem [6+2] ene type reaction
A model study is described on a new approach to the synthesis of diquinane and angular triquinane systems, via iron-promoted tandem [6+2] ene-type double cyclization followed by ozonolysis and intramolecular aldol reaction. [Display omitted]
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Published in: | Tetrahedron 2010-07, Vol.66 (27), p.4943-4946 |
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Main Authors: | , , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | A model study is described on a new approach to the synthesis of diquinane and angular triquinane systems, via iron-promoted tandem [6+2] ene-type double cyclization followed by ozonolysis and intramolecular aldol reaction.
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ISSN: | 0040-4020 1464-5416 |
DOI: | 10.1016/j.tet.2010.05.018 |